Canonical Allele Identifier: CA1428759363
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404801A= , CM000665.2:g.190404801A= GRCh38
NC_000003.11:g.190122590A= , CM000665.1:g.190122590A= GRCh37
NC_000003.10:g.191605284A= NCBI36
NG_008149.1:g.21750A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.257A= MANE Select ENSP00000264734.3:p.Asp86=
ENST00000456423.2:c.115-5102A= ENSP00000414136.2:n.115-5102A=
ENST00000264734.2:c.467A= ENSP00000264734.2:p.Asp156=
ENST00000456423.1:c.325-5102A= ENSP00000414136.1:n.325-5102A=
ENST00000468220.1:n.449A=
NM_006580.3:c.467A= NP_006571.1:p.Asp156=
NM_001378492.1:c.257A= NP_001365421.1:p.Asp86=
NM_001378493.1:c.257A= NP_001365422.1:p.Asp86=
NM_006580.4:c.257A= MANE Select NP_006571.2:p.Asp86=